Evidence map›Paper›PMID 19537844›Full record

ReviewMolecular diagnosis & therapy2009

Diagnostic microarrays in hematologic oncology: applications of high- and low-density arrays.

Tatyana V Nasedkina, Natalia A Guseva, Olga A Gra, Olga N Mityaeva, Alexander V Chudinov, Alexander S Zasedatelev

Abstract readReview
PubMed Publisher
In one paragraph

Review in Molecular diagnosis & therapy, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.9field-weighted citation impact, top 27% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Tatyana V NasedkinaEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow, Russia. nased@eimb.ru
Natalia A Guseva
Olga A Gra
Olga N Mityaeva
Alexander V Chudinov
Alexander S Zasedatelev
Russian Academy of Sciences · RUEngelhardt Institute of Molecular Biology · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Microarrays have become important tools for high-throughput analysis of gene expression, chromosome aberrations, and gene mutations in cancer cells. In addition to high-density experimental microarrays, low-density, gel-based biochip technology represents a versatile platform for translation of research into clinical practice. Gel-based microarrays (biochips) consist of nanoliter gel drops on a hydrophobic surface with different immobilized biopolymers (primarily nucleic acids and proteins). Because of the high immobilization capacity of the gel, such biochips have a high probe concentration and high levels of fluorescence signals after hybridization, which allow the use of simple, portable detection systems. The notable accuracy of the analysis is reached as a result of the high level of discrimination between positive and negative gel-bound probes. Different applications of biochips in the field of hematologic oncology include analysis of chromosomal translocations in leukemias, diagnostics of T-cell lymphomas, and pharmacogenetics.

Indexed as

Biomarkers, TumorChromosome AberrationsGene RearrangementGenes, T-Cell Receptor gammaHematologic NeoplasmsHumansLeukemiaOligonucleotide Array Sequence AnalysisPolymorphism, Single NucleotideProtein Array AnalysisBiomarkers, Tumor

Identifiers

PMID19537844
OpenAlexW225603108

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.